Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
500 participants
OBSERVATIONAL
2020-01-01
2026-12-31
Brief Summary
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Detailed Description
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1. To evaluate the impact of FFR on decision for PCI in ACS patients
2. To assess the long term prognosis of deferring PCI based on FFR value in non-culprit lesion; defying the cut-off value of FFR for PCI in the non-culprit lesion of ACS patients
3. To identify the relation between OCT findings and FFR value in culprit and non-culprit lesions of ACS patients
4. To compare the long term prognosis of PCI or deferring PCI based on FFR value in non-culprit lesion of ACS patients
5. To identify OCT findings to predict the lesion progression in deferred lesions.
6. To assess the long term prognosis of post-PCI FFR value in the culprit lesion of NSTE-ACS patients
7. To assess the efficacy of routine use of FFR to guide PCI in ACS patients; angiographically guidance versus FFR guidance
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Fractional Flow Reserve
Functional assessement of anatomical stenosis of coronary artery
Eligibility Criteria
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Inclusion Criteria
* Diagnosed as ACS (unstable angina/ Non ST elevation myocardial infarction, ST elevation myocardial infarction)
* At least one stenosis of \>50% in a non-culprit vessel ≥ 2.0 mm by visual estimation with TIMI 3 - multivessel disease after PCI for culprit lesion or single vessel disease with ambiguity for PCI ④ FFR within hospitalization for index PCI for ACS
Exclusion Criteria
* Cardiogenic shock (Killip class IV) already at presentation or the completion of culprit PCI
* Intolerance to Aspirin, Clopidogrel, Prasugrel, Ticagrelor, Heparin, Bivaluridin, or Everolimus
* Known true anaphylaxis to contrast medium (not allergic reaction but anaphylactic shock)
⑤ Pregnancy or breast feeding
⑥ Non-cardiac co-morbid conditions are present with life expectancy \<1 year or that may result in protocol noncompliance (per site investigator's medical judgment).
⑦ Other primary valvular disease with severe degree: severe mitral regurgitation or mitral stenosis, severe aortic regurgitation or aortic stenosis
⑧ Patients with a history of Coronary Artery Bypass Graft(CABG)
⑨ Unwillingness or inability to comply with the procedures described in this protocol.
19 Years
85 Years
ALL
No
Sponsors
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The Catholic University of Korea
OTHER
Responsible Party
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Eun Ho Choo
Assistant Professor
Principal Investigators
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Eun Ho Choo, M.D.,PhD
Role: PRINCIPAL_INVESTIGATOR
The Catholic University of Korea
Locations
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St.Vincent's Hospital
Suwon, Gyeonggido, South Korea
Uijeongbu St.Mary's Hospital
Uijeongbu-si, Gyeonggido, South Korea
Daejeon St.Mary's Hospital
Daejeon, , South Korea
Incheon St.Mary's Hospital
Incheon, , South Korea
The Catholic University of Korea Seoul St. Mary's Hospital
Seoul, , South Korea
Countries
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Other Identifiers
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PressureACS
Identifier Type: -
Identifier Source: org_study_id
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